Senior Statistical Programmer

Description

At Bristol Myers Squibb, our employees often ask, “Who are you working for?”—a question that fuels collaboration, accountability, and urgency in our work. Our purpose-driven culture inspires us to discover, develop, and deliver innovative medicines to prevail over serious diseases. We offer uniquely interesting and meaningful work, opportunities for growth, and a supportive environment that values inclusion, wellbeing, flexibility, and comprehensive benefits. This is work that transforms the lives of patients, and the careers of those who do it.

Responsibilities

• Writing and validating SAS programs to generate derived analysis datasets and clinical Tables, Figures, and Listings (TFLs) - work that feeds directly into regulatory decision-making
• Contributing to electronic submission preparation (think NDA, BLA, MAA ) — real regulatory milestones that mark pivotal moments in a medicine's journey
• Reviewing and shaping key planning documents like Statistical Analysis Plans (SAPs) and Data Presentation Plans , ensuring clarity and completeness before programming work begins - your input genuinely steers project direction
• Partnering with vendors on programming standards, specifications, and file transfers , building the kind of collaborative relationships that make complex programmes run smoothly
• Independently leading programming assignments across multiple projects with minimal supervision - you'll have real ownership and the trust to match it
• Spotting opportunities to improve efficiency and consistency across GBDS, contributing to initiatives that make the whole team better
• What you bring to the table
• We're looking for someone with a solid foundation and the drive to apply it meaningfully. Here's what we need:
• Education & Background
• A Bachelor's degree in Statistics, Biostatistics, Mathematics, Computer Science, or Life Sciences
• Demonstrated industry experience in statistical programming
• Core Skills & Knowledge
• Strong, proven proficiency in SAS for producing derived analysis datasets and TFLs
• In-depth understanding of clinical data structures , including CDISC standards (SDTM, ADaM) and relational databases
• Hands-on experience with upstream data handling - multiple data forms, eDC , workflow, and SDTM
• Ability to deliver downstream outputs including ADaM datasets, Data Definition Tables, and e-submission packages
• Confidence with tools like MS Office, XML and Pinnacle 21
• A solid grasp of regulatory, industry, and technology standards - you understand why the rules exist, not just what they are
• Familiarity with statistical terminology, clinical trial methodology, medical terminology, and protocol designs
• A genuine team player - you communicate well, build bridges across functions, and make the people around you more effective
• It'd be a bonus if you also have…
• Deep experience supporting global regulatory filings (NDA, BLA, MAA) within pharma clinical development
• Broad knowledge of the end-to-end drug development process and global regulatory frameworks
• Experience with R or other statistical programming languages
• Familiarity with the Linux operating system
• Why this role, why BMS, why now?
• Here, your skills aren't just technically valued - they're mission critical . You'll work in an environment that respects your expertise, gives you the autonomy to lead your own work, and connects your daily output to outcomes that genuinely matter.
• You'll gain:
• Exposure to the full clinical development lifecycle , from data collection through to regulatory submission
• The chance to work with industry-leading standards and technologies in a global biometrics function
• A culture that actively encourages you to identify improvements and champion change - your ideas won't gather dust here
• Collaboration with talented, purpose-driven colleagues across global cross-functional teams
• LI-Hybrid
• We hire for skills and capabilities, not just credentials – if this role excites you, but doesn’t perfectly match your resume, we encourage you to apply anyway.

Conditions

Hybrid Working: 50% Onsite

Are you ready to turn clinical data into life-changing decisions?

At Bristol Myers Squibb , we believe that behind every dataset, every line of code, and every submission package, there's a patient waiting for a better option. As our Senior Statistical Programmer , you are one of the people who makes that happen.

This isn't a role where your work disappears into a black box. Here, your programming expertise directly shapes how new medicines are developed, reviewed by regulators, and ultimately approved for patients around the world. That's a pretty remarkable thing to be part of.

What you'll actually be doing

You'll be a key technical voice within our Global Biometrics & Data Sciences (GBDS) function, working closely with cross-functional clinical teams, collaborating with external vendors, and owning your programming workload with real autonomy.

This is a focused individual contributor role - no line management responsibilities — so you can put your energy exactly where it matters most: delivering high-quality, high-impact programming work.

Where you work matters – because collaboration, innovation and patient impact happen in many settings. Our roles are structured across four work models: site-essential, site-by-design, field-based and remote-by-design. The model assigned to this role is based on its core responsibilities. Learn more at https://careers.bms.com/ways-of-working .

Supporting People with Disabilities

BMS is dedicated to ensuring that people with disabilities can excel through a transparent recruitment process, reasonable workplace accommodations/adjustments and ongoing support in their roles. Applicants can request a reasonable workplace accommodation/adjustment prior to accepting a job offer. If you require reasonable accommodations/adjustments in completing this application, or in any part of the recruitment process, direct your inquiries to adastaffingsupport@bms.com . Visit careers.bms.com/eeo-accessibility to access our complete Equal Employment Opportunity statement.

Bristol Myers Squibb is Disability Confident – Employer

A UK Government scheme

Candidate Rights

BMS will consider qualified applicants with arrest and conviction records, pursuant to applicable laws in your area.

For roles based in Los Angeles County only: If you live in or expect to work from Los Angeles County if hired for this position, please visit this page for important additional information: https://careers.bms.com/california-residents/

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R1604799 : Senior Statistical Programmer